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T细胞发育、激活及信号转导的分子见解(综述)

Molecular insights into T cell development, activation and signal transduction (Review).

作者信息

Omar Isra, Alakhras Ahmed, Mutwali Samahir, Bakhiet Moiz

机构信息

Department of Clinical Medicine, College of Medicine, Almaarefa University, 11597 Riyadh, Kingdom of Saudi Arabia.

Department of Clinical Medicine, College of Medicine, University of Medical Sciences and Technology, 3523 Kigali, Rwanda.

出版信息

Biomed Rep. 2025 Apr 7;22(6):94. doi: 10.3892/br.2025.1972. eCollection 2025 Jun.

Abstract

T cell modulation plays a fundamental role to adaptive and innate immunity, which aids the recognition and defense against pathogens while also maintaining self-tolerance. Numerous molecular pathways participate in this process including thymic selection, T cell receptor and antigen-presenting cells cross linkage, along with co-stimulatory signaling cascades. The present review demonstrates a holistic analysis of various classic and novel mechanisms that govern T cell regulation and emerging therapeutic applications. Recent advancements have introduced novel roles in the journey of T cell modulation that can have a pivotal impact on the understanding of this process; for example, phase separation of the linker for activation of T cells, and the newer application of chimeric antigen receptor (CAR) T cell therapy in autoimmune diseases. While discoveries of proximal and distal signal transduction pathways have contributed to the comprehension of T cell anergy, cytokine-mediated differentiation and the delicate balance between immune activation and tolerance, there are still unresolved debates about further molecular mechanisms. There are also still questions about the long-term side effects of CAR-T cell therapy. Deeper research and analysis are required to further aid the understanding and use of this novel therapeutic approach.

摘要

T细胞调节在适应性免疫和固有免疫中发挥着基础性作用,有助于识别和抵御病原体,同时维持自身耐受性。众多分子途径参与这一过程,包括胸腺选择、T细胞受体与抗原呈递细胞的交联,以及共刺激信号级联反应。本综述对调控T细胞调节的各种经典和新型机制以及新兴治疗应用进行了全面分析。最近的进展在T细胞调节过程中引入了新的作用,这可能对理解这一过程产生关键影响;例如,T细胞激活连接蛋白的相分离,以及嵌合抗原受体(CAR)T细胞疗法在自身免疫性疾病中的新应用。虽然近端和远端信号转导途径的发现有助于理解T细胞无反应性、细胞因子介导的分化以及免疫激活与耐受之间的微妙平衡,但关于进一步的分子机制仍存在未解决的争论。关于CAR-T细胞疗法的长期副作用也仍然存在疑问。需要更深入的研究和分析,以进一步帮助理解和应用这种新型治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8442/12001230/3838cdc39f06/br-22-06-01972-g00.jpg

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